4.6 Article

The Amino Acid Sequences Flanking an Antigenic Determinant Can Strongly Affect MHC Class I Cross-Presentation without Altering Direct Presentation

Journal

JOURNAL OF IMMUNOLOGY
Volume 182, Issue 8, Pages 4601-4607

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.0803806

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Funding

  1. NCI NIH HHS [P30 CA006927, P30 CA006927-46, CA006927] Funding Source: Medline
  2. NIAID NIH HHS [R21 AI058179-02, R21AI058179, R01 AI048849, R01 AI048849-08, R01AI048849, R21 AI058179] Funding Source: Medline

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Direct presentation (DP) and cross presentation (CP) on MHC I by professional APCs are defined by the internal or external source of the Ag, respectively. Although some Ags are substrates for both DP and CP, others are only substrates for DIP. The reasons for this difference remain largely unknown. In this study, we studied in tissue culture and also in vivo, the effects of altering the length and sequence of the amino acid chains flanking an MHC class I restricted determinant (the chicken OVA OVA(258-265), SIINFEKL) that is normally a good substrate for both DP and CP. We demonstrate that CP but not DP strictly requires flanking N and C-terminal extensions of minimal length. Furthermore, we show that removal but not replacement of just one amino acid 22 residues downstream from the determinant is sufficient to strongly affect CP without affecting either protein stability or DP. Thus, our work shows that the flanking residues of an antigenic determinant can differentially affect CP and DP, and that features of the Ag other than half-life can have a major impact in CP. Our studies may have implications for understanding CP in viral infections and possibly for the design of new vaccines. The Journal of Immunology, 2009, 182: 4601-4607.

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